Palladium-catalyzed cycloaddition of carbon dioxide with methoxyallene

A palladium catalyst generated from Pd₂(dba)₃·CHCl₃ and ⁿBu₂PCH₂CH₂Py (Py = 2-pyridyl) has effected novel cycloaddition of methoxyallene with CO₂ to afford (E)-5-methoxy-2-(methoxy-methylene)-4-methylene-5-pentanolide regio- and stereospecifically, where a methoxy functional group plays an important role.     

The vinylogous intramolecular Morita-Baylis-Hillman reaction: synthesis of functionalized cyclopentenes and cyclohexenes with trialkylphosphines as nucleophilic catalysts

The development of the vinylogous intramolecular Morita-Baylis-Hillman reaction for the synthesis of functionalized cyclopentenes and cyclohexenes is described. The reaction involves the trialkyphosphine-catalyzed cyclization of 1,6- or 1,7-diactivated 1,5-hexadienes or 1,6-heptadienes, containing carboxyaldehyde, methyl ketone, or methoxycarbonyl as the olefin activating groups. A representative example of this reaction is the Me(3)P-catalyzed cyclization of 1a in tert-amyl alcohol, which provides the substituted cyclopentene 2a in 95% yield and with 97:3 regioselectivity.     

Novel carbon-carbon bond formation reaction of methoxyallene oxide promoted by TiI(4)

Methoxyallene oxide was readily prepared in situ by epoxidation of methoxyallene with 3-chloroperbenzoic acid, and the subsequent reaction with aldehydes or acetals was promoted by titanium tetraiodide and additives to give 2,3-dialkoxy- or 3-hydroxy-2-methoxy ketones in good yields.     

Stabilization of reaction products of ureas with polyfluoro ketones

Conclusions Polyfluorinated tetrahydro-1,3,5-oxadiazine derivatives were obtained by the condensation of urea and thiourea with polyfluoro ketones.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2168–2169, September, 1977.     

Stabilization of the enol form of ketones by the isothiuronium group

A. N. Nesmeyanov Institute of Organometallic Compounds, Russian Academy of Sciences, 317813 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 10, pp. 2459–2460, October, 1992.     

Conductometric titration study of the reactions of some trialkylphosphines with bromine,iodine and iodine bromide

The reactions of tributyl-, trioctyl-, and tricyclohexyl-phosphine with bromine, iodine and iodine bromide have been studied by conductometric titration in acetonitrile. In general, evidence was obtained for the formation, in solution, of highly conducting 0.5 : 1, 1 : 1, and 2 : 1 adducts. The 1 : 1 and 2 : 1 adducts (R₃PX₂ and R₃PX₄) were isolated and the electrolytic conductivity of their acetonitrile solutions measured. Values of molar conductivity are reported; these point to strong electrolyte behaviour, hence the 1 : 1 and 2 : 1 adducts must be formulated as the phosphonium salts, R₃PX⁺X^? and R₃PX⁺X₃^? respectively.     

New possibilities for the use of methoxyallene in carbon-carbon bond-forming reactions

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 198–199, January, 1988.     

Stabilization of the N-1-substituted cytosinate iminooxo form in dinuclear palladium complexes

The synthesis, as well as chemical and structural characterization, of 1-(p-toluenesulfonyl)cytosine (1) and its dinuclear complexes of the composition Pd₂(1-TosC^?–N3,N4)₄ (3) and Pd₂(1-TosC^?–N3,N4)₂DMSO₂Cl₂ (4) by means of ESI-MS, IR, ¹H NMR and X-ray single crystal analysis are described. Ligand 1 exists in the preferred aminooxo tautomeric form, while both dinuclear complexes reveal the presence of the iminooxo form of the ligand, where 1-TosC^? stands for the anion of the cytosine derivative of 1, bridging two palladium atoms. Complex 3 has a paddlewheel structure with two square-planar coordination spheres, consisting of four N atoms each, mutually parallel and perpendicular to the interpalladium vector. Complex 4 is characterized by two mutually parallel square-planar coordination spheres consisting of two nitrogens, sulfur from the solvent molecule and a chloride. A feasible chemical route for the formation of 3 and 4 via the kinetically favoured mononuclear complex Pd(1-TosC–N3)₂Cl₂ (2) is proposed, based on the IR, ¹H NMR, mass spectrometry, elemental analysis and X-ray structure analysis data.     

Stabilization of CoI by ZnII in pure acetonitrile and its reaction with aryl halides

The study of the electrochemical behavior of cobalt(II) bromide (CoBr(2)) in pure acetonitrile allowed us to demonstrate that Co(2+) is the catalyst precursor involved in the electrochemical and chemical conversions of arylhalides, ArX, to arylzinc compounds in that solvent. The reduction of Co(2+) leads to the Co(+) species, which disproportionates too rapidly to react further with aryl halides. However, the presence of zinc(II) bromide allows us to stabilize the electrogenerated cobalt(I) and to observe it on the timescale of slow cyclic voltammetry. Under such conditions, the Co(I) species has time to react with aryl halides and produce [Co(III)ArX](+) complexes that are reduced into [Co(II)ArX] by a single electron uptake at the same potential at which Co(2+) is reduced. Rate constants for the oxidative addition of ArX to Co(I) have been determined for various aryl halides and compared to the values obtained in an acetonitrile (ACN)/pyridine (9:1, v/v) mixture. It is shown that Co(I) is stabilized more by ZnBr(2) than by pyridine. A transmetallation reaction between [Co(II)ArX] and ZnBr(2) has also been observed. We finally propose a mechanism for the cobalt-catalyzed electrochemical conversion of aryl bromides into organozinc species in pure acetonitrile.     

Samarium diiodide-induced couplings of carbonyl compounds with methoxyallene leading to 4-hydroxy 1-enol ethers

A surprising samarium diiodide-induced coupling reaction of carbonyl compounds with methoxyallene provided 4-hydroxy 1-enol ethers, which are versatile synthetic building blocks. In this coupling reaction, methoxyallene serves as an acrolein equivalent, which cannot directly be employed. [reaction: see text]     

Zwitterionic sulfobetaine lipids that form vesicles with salt-dependent thermotropic properties

We describe a class of zwitterionic sulfobetaine (SB) lipids with fascinating salt-dependent properties. SB lipids are zwitter-neutral across a broad pH range; however they have negative surface potentials in the presence of anions and two salt-dependent transition temperatures. These new SB lipids provide insight on the role of charge orientation at the membrane interface and may be useful components in drug delivery systems.     

Stabilization effect of single-walled carbon nanotubes on the functioning of photosynthetic reaction centers

The interaction between single-walled carbon nanotubes and photosynthetic reaction centers purified from purple bacterium Rhodobacter sphaeroides R-26 has been investigated. Atomic force microscopy studies provide evidence that reaction center protein can be attached effectively to the nanotubes. The typical diameter of the nanotube is 1-4 nm and 15 +/- 2 nm without and with the reaction centers, respectively. Light-induced absorption change measurements indicate the stabilization of the P+(Q(A)Q(B))- charge pair, which is formed after single saturating light excitation after the attachment to nanotubes. The separation of light-induced charges is followed by slow reorganization of the protein structure. The stabilization effect of light-initiated charges by the carbon nanotubes opens a possible direction of several applications, the most promising being in energy conversion and storage devices.     

Domino reactions that combine an azido-Schmidt ring expansion with the Diels-Alder reaction

[reaction: see text] The combination of the intramolecular Schmidt reaction with the Diels-Alder reaction provides expedient access to a variety of heterocycles. Two different modes of reaction planning are presented. In one, the azide and ketone moieties necessary for the intramolecular Schmidt reaction originate on different molecules that are reacted and subsequently undergo a ring-adjustment step. Alternatively, an azido ketone can be used provided the ketone is deactivated by its presence in an enone.     

Aromatic oligomers that form hetero duplexes in aqueous solution

The electron-deficient 1,4,5,8-naphthalenetetracarboxylic diimide (Ndi) and electron-rich 1,5-dialkoxynaphthalene (Dan) have been shown to complex strongly with each other in water due to the hydrophobic effect as modulated through the electrostatic complementarity of the stacked dimer. Previously, oligomers of alternating Ndi and Dan units, termed aedamers, were the first foldamers to employ intramolecular aromatic stacking to effect the formation of secondary structure of nonnatural chains in aqueous solution. Described here is the use of this aromatic-aromatic (or pi-pi) interaction, this time in an intermolecular format, to demonstrate the self-assembly of stable hetero duplexes from a set of molecular strands (1a-4a) and (1b-4b) incorporating Ndi and Dan units, respectively. A 1-to-1 binding stoichiometry was determined from NMR and isothermal titration calorimetry (ITC) investigations, and these experiments indicated that association is enthalpically favored with the tetra-Ndi (4a) and tetra-Dan (4b) strands forming hetero duplexes (4a:4b) with a stability constant of 350 000 M-1 at T = 318 K. Polyacrylamide gel electrophoresis (PAGE) also illustrated the strong interaction between 4a and 4b and support a 1-to-1 binding mode even when one component is in slight excess. Overall, this system is the first to utilize complementary aromatic units to drive discrete self-assembly in aqueous solution. This new approach for designing assemblies is encouraging for future development of duplex systems with highly programmable modes of binding in solution or on surfaces.     

Assignment of the 13C NMR resonances in trialkylphosphines from spin-lattice relaxation time measurements

Analysis of the ¹³C NMR chemical shift and coupling constant data for a number of straight-chain aliphatic trialkylphosphines and their transition metal carbonyl complexes suggests that complexation leads to: (1) a deshielding of C(1) and an increase in ¹J(¹³C³¹P), (2) a slight shielding of C(2) and a decrease in ²J(¹³C³¹P), and (3) little or no change in the chemical shift for C(3) and a slight increase in ³J(¹³C³¹P). Application of these rules to the assignment of the ¹³C NMR spectrum of P(butyl)₃ led to conflict with prior work. A study of segmental motion in these derivatives via spin-lattine (T₁) relaxation time measurements was therefore performed, and these data are in complete agreement with the proposed assignments. These generalizations must be applied with care, however, since the presence of either unsaturation or branching near the phosphorus can interfere with this pattern.     

Stabilization of antioxidant gallate in layered double hydroxide by exfoliation and reassembling reaction

As for the stabilization of chemically sensitive bioactive molecule in this study, gallic acid (GA) with antioxidant property was intercalated into interlayer space of layered double hydroxide (LDH), which was realized by exfoliation and reassembling reaction. At first, the pristine nitrate-type Zn₂Al-LDH in solid state was synthesized via co-precipitation followed by the hydrothermal treatment at 80 °C for 6 h, and then exfoliated in formamide to form a colloidal solution of exfoliated LDH nanosheets, and finally reassembled in the presence of GA to prepare GA intercalated LDH (GA-LDH) desired, where the pH was adjusted to 8.0 in order to deprotonate GA to form gallate anion. According to the XRD analysis, GA-LDH showed well-developed (00l) diffraction peaks with a basal spacing of 1.15 nm, which was estimated to be larger than that of the pristine LDH (0.88 nm), indicating that gallate molecules were incorporated into LDH layers with perpendicular orientation. From the FT-IR spectra it was found that gallic acid was completely deprotonated into gallate, and stabilized in between LDH lattices via electrostatic interaction. The content of GA in GA-LDH was determined to be around 23 wt% by UV–vis spectroscopic study, which was also confirmed by HPLC analysis. According to the in-vitro release of GA out of GA-LDH in PBS solution (pH 7.4) at 4 °C, GA was sustainably released from GA-LDH nanohybrid up to 86% within 72 h. The antioxidant property of GA-LDH was almost the same with that of intact GA which was examined by DPPH. The photostability of GA-LDH under UV light irradiation was immensely enhanced compared to intact GA. It is, therefore, concluded that the present GA-LDH nanohybrid can be considered as an excellent antioxidant material with high chemical- and photo-stabilities, and controlled release property.     

The key intermediates that interact with the fluorophores in the peroxyoxalate chemiluminescence reaction of 2,4,6-trichlorophenyl N-aryl-N-tosyloxamates

A kinetic study of peroxyoxalate chemiluminescence reactions employing 2,4,6-trichlorophenyl N-aryl-N-tosyloxamates supports the 1,2-dioxetanones still bearing the eliminating group as the key intermediates that interact with the fluorophores rather than 1,2-dioxetanedione.     

Off-line form of the Michaelis-Menten equation for studying the reaction kinetics in a polymer microchip integrated with enzyme microreactor

We firstly transformed the traditional Michaelis-Menten equation into an off-line form which can be used for evaluating the Michaelis-Menten constant after the enzymatic reaction. For experimental estimation of the kinetics of enzymatic reactions, we have developed a facile and effective method by integrating an enzyme microreactor into direct-printing polymer microchips. Strong nonspecific adsorption of proteins was utilized to effectively immobilize enzymes onto the microchannel wall, forming the integrated on-column enzyme microreactor in a microchip. The properties of the integrated enzyme microreactor were evaluated by using the enzymatic reaction of glucose oxidase (GOx) with its substrate glucose as a model system. The reaction product, hydrogen peroxide, was electrochemically (EC) analyzed using a Pt microelectrode. The data for enzyme kinetics using our off-line form of the Michaelis-Menten equation was obtained (K(m) = 2.64 mM), which is much smaller than that reported in solution (K(m) = 6.0 mM). Due to the hydrophobic property and the native mesoscopic structure of the poly(ethylene terephthalate) film, the immobilized enzyme in the microreactor shows good stability and bioactivity under the flowing conditions.     

An analysis of the difficulties associated with determining that a reaction in chemical equilibrium is incomplete

Foundations of Chemistry - There are inherent difficulties in a subject like chemistry particularly the notion of a chemical reaction. In this paper the difficulties are discussed from a teaching...